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Effects of exercise training and vitamin D supplementation on Migraine

Effects of 8 weeks of aerobic exercise and vitamin D supplementation on serum levels of brain-derived neurotrophic factor, quality of life, and some cognitive and psychological indices in Migraine patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210617051606N3
Enrollment
48
Registered
2021-10-27
Start date
2021-10-07
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Migraine without aura. Migraine without aura

Interventions

Intervention 1: Intervention group: continuous aerobic exercise for 8 weeks and 3 sessions per week. In the first week, the duration of training will be 20 minutes and the intensity will be 50% of hea

Sponsors

Razi University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Not participation in regular exercise over the last 6 months Having Migraine without aura confirmed by a specialist Getting the certification of no prohibition of participating in the exercise training program from a specialist Insufficient values of Vitamin D (20-29 nanograms/milliliter) Aged between 20 to 50 years

Exclusion criteria

Exclusion criteria: Any psychiatric disorders other than Migraine without aura Alcohol and other kinds of drug addiction Musculoskeletal disorder Cardiovascular and pulmonary diseases Refusal to give informed consent

Design outcomes

Secondary

MeasureTime frame
Changes in depression severity. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: By the use of Beck’s Depression Inventory.;Change in the quality of sleep. Timepoint: Before intervention and after 8 weeks of intervention. Method of measurement: Pittsburgh Sleep Quality Index.;Change in physical self-concept. Timepoint: Before intervention and after 8 weeks of intervention. Method of measurement: Physical self-concept questionnaire.

Primary

MeasureTime frame
Change in serum levels of brain-derived neurotrophic factor. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: By the use of blood sample and ELISA method.;Change in quality of life. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: World health organization standard quality of life questionnaire (short version).;Changes in severity, duration, and frequency of Migraine attacks. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: By the use of researcher-made questionnaire to record the pertinent variables of Migraine attacks.;Changes in memory performance. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: By the use of Subjective Memory Complaints Scale.;Changes in cognitive performance. Timepoint: Before starting the intervention, and 8 weeks after starting the intervention. Method of measurement: By the use of Ascertain Dementia 8 (AD8) questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEhsan Amiri

Razi University

e.amiri@razi.ac.ir+98 83 3845 8428

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026